根治性前列腺切除术后PSA持续和复发的发生率和预后意义。以人群为基础的研究

Pietro Scilipoti, Hans Garmo, Rolf Gedeborg, David Robinson, Pär Stattin, Marcus Westerberg
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Results Among 10,700 men, the 10-year risk of PSA persistence or relapse after RP was 34% (95% CI, 32-35%). Within 12 months of persistence/relapse, 75% of men with persistence, high-risk relapse or early relapse (<2 years) received treatment. The 10-year risk of PCa death ranged from 12% for men with persistence to 2% in men with low-risk relapse, while death from other causes ranged from 11% to 16%. Risk of PCa death was 8.5% after early relapse (<2 years) and 1.4% after late relapse (>5 years). Conclusions This population-based study estimated that one third of men would have PSA persistence or relapse within 10 years from RP. There was a wide range in risk of death from PCa according to cancer characteristics and time to relapse. Risk of death from other causes was substantial. 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摘要

前列腺癌(PCa)根治性前列腺切除术(RP)后前列腺特异性抗原(PSA)持续和复发的发生率广泛。我们的目的是描述PSA持续和复发的发生率和预后意义。方法在瑞典对2007年至2020年间诊断为PCa并接受RP的男性进行登记队列研究。使用竞争风险累积发生率曲线估计风险。根据持久性、欧洲泌尿外科协会复发风险组、复发时间和基于年龄和合共病的预期寿命,对持续或复发后的治疗、PCa死亡风险和其他原因进行分层。结果在10,700名男性中,RP后PSA持续或复发的10年风险为34% (95% CI, 32-35%)。在持续/复发12个月内,75%的持续、高危复发或早期复发(2年)的男性接受了治疗。前列腺癌患者的10年死亡风险从持续患者的12%到低风险复发患者的2%不等,而其他原因导致的死亡风险从11%到16%不等。早期复发(2年)后前列腺癌死亡风险为8.5%,晚期复发(5年)后死亡风险为1.4%。结论:这项基于人群的研究估计,三分之一的男性在RP后10年内PSA持续存在或复发。根据癌症特征和复发时间,前列腺癌的死亡风险范围很大。其他原因造成的死亡风险很大。这些因素,连同预期寿命,应该为男性持续或复发的治疗决策提供信息。
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Incidence and prognostic implications of PSA persistence and relapse after radical prostatectomy. Population-based study
Background There has been a wide range in incidence of prostate-specific antigen (PSA) persistence and relapse after radical prostatectomy (RP) for prostate cancer (PCa). We aimed to describe incidence and prognostic implications of PSA persistence and relapse. Methods Register-based cohort study in Sweden of men diagnosed with PCa between 2007 and 2020 who underwent RP. Risks were estimated using competing risk cumulative incidence curves. Treatment after persistence or relapse and risk of PCa death and other causes were stratified according to persistence, European Association of Urology relapse risk groups, time to relapse, and life expectancy based on age and comorbidities. Results Among 10,700 men, the 10-year risk of PSA persistence or relapse after RP was 34% (95% CI, 32-35%). Within 12 months of persistence/relapse, 75% of men with persistence, high-risk relapse or early relapse (<2 years) received treatment. The 10-year risk of PCa death ranged from 12% for men with persistence to 2% in men with low-risk relapse, while death from other causes ranged from 11% to 16%. Risk of PCa death was 8.5% after early relapse (<2 years) and 1.4% after late relapse (>5 years). Conclusions This population-based study estimated that one third of men would have PSA persistence or relapse within 10 years from RP. There was a wide range in risk of death from PCa according to cancer characteristics and time to relapse. Risk of death from other causes was substantial. These factors, along with life expectancy, should inform treatment decisions for men with persistence or relapse.
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